Song Zewen, Zhang Xi, Ma Yechen, Ma Shuyun, Feng Ziyang, Liu Xuewen
Department of Oncology, The Third Xiangya Hospital of Central South University, Changsha, PR China.
Department of Oncology, The Third Xiangya Hospital of Central South University, Changsha, PR China.
Transl Oncol. 2025 Jan;51:102184. doi: 10.1016/j.tranon.2024.102184. Epub 2024 Nov 2.
To evaluate the efficacy and the incidence of symptomatic radiation pneumonitis (RP) of the adaptive radiation strategy with V20 limitation in stage III non-small cell lung cancer (NSCLC) patients receiving concurrent immunotherapy and radiotherapy Materials and Methods: We retrospectively reviewed stage III NSCLC patients received thoracic radiation with or without immunotherapy from January 2015 to September 2024 in the Third Xiangya Hospital. The overall survival (OS), progression free survival (PFS), objective response rate (ORR), and the incidence of symptomatic RP were compared among patients stratified by the sequential of immunotherapy and radiotherapy.
45 patients received concurrent immunotherapy and radiotherapy with application of the adaptive radiation strategy (the CIR group). 32 patients received simultaneous integrated boost intensity-modulated radiotherapy (SIB-IMRT), 26 patients received 2 to 4 cycles neoadjuvant immuno-chemotherapy before the concurrent immunotherapy and radiotherapy, 7 patients received thoracic radiotherapy with a prescribed dosage of 50 Gy, and 10 patients received radiotherapy with CTV omission. 86.67 % (39/45) patients had a V20 ≤ 20 %. The ORR was 86.67 %. The median PFS of these patients was significantly longer than those received concurrent chemo-radiotherapy followed by immunotherapy (the PACIFIC paradigm, HR, 2.40; 95 % CI, 1.15 to 5.02; log-rank p = 0.013; median, 28.6 vs. 16.1 months p = 0.013). The median OS was not reached. 13.3 % patients in the CIR group experienced grade ≥ 2 RP and the incidence was significantly lower than that of patients received radiotherapy without immunotherapy or concurrent chemo-radiotherapy with immunotherapy consolidation.
The application of adaptive radiotherapy strategies with V20 limitation demonstrated robust antitumor activity and reduced pulmonary toxicity in stage III NSCLC patients receiving concurrent ICIs treatment and thoracic radiation. This treatment modality deserves further validation as a promising therapy in patients with treatment-naive, unresectable, stage III NSCLC.
评估序贯免疫治疗和放疗的时机对接受同步免疫治疗和放疗的III期非小细胞肺癌(NSCLC)患者采用V20限制的自适应放疗策略的疗效及放射性肺炎(RP)症状发生率。材料与方法:回顾性分析2015年1月至2024年9月在中南大学湘雅三医院接受胸部放疗(无论是否联合免疫治疗)的III期NSCLC患者。比较按免疫治疗和放疗顺序分层的患者的总生存期(OS)、无进展生存期(PFS)、客观缓解率(ORR)及RP症状发生率。
45例患者接受同步免疫治疗和放疗并采用自适应放疗策略(CIR组)。32例患者接受同步整合加量调强放疗(SIB-IMRT),26例患者在同步免疫治疗和放疗前接受2至4周期新辅助免疫化疗,7例患者接受处方剂量为50 Gy的胸部放疗,10例患者接受CTV遗漏放疗。86.67%(39/45)的患者V20≤20%。ORR为86.67%。这些患者的中位PFS显著长于接受同步放化疗后序贯免疫治疗的患者(PACIFIC模式;HR,2.40;95%CI,1.15至5.02;对数秩检验p = 0.013;中位值,28.6个月对16.1个月;p = 0.013)。中位OS未达到。CIR组13.3%的患者发生≥2级RP,发生率显著低于未接受免疫治疗的放疗患者或同步放化疗联合免疫治疗巩固的患者。
在接受同步免疫检查点抑制剂(ICI)治疗和胸部放疗的III期NSCLC患者中,采用V20限制的自适应放疗策略显示出强大的抗肿瘤活性并降低了肺部毒性。作为一种有前景的治疗方法,这种治疗模式值得在初治、不可切除的III期NSCLC患者中进一步验证。